Serum Soluble Interleukin-2 Receptor as a Potential Biomarker for Immune-related Adverse Events

Anticancer Res. 2021 Feb;41(2):1021-1026. doi: 10.21873/anticanres.14857.

Abstract

Background/aim: Biomarkers for immune-related adverse events (irAEs) induced by immune checkpoint inhibitors (ICIs) are required. We encountered a patient whose skin irAE fluctuated in parallel with serum soluble interleukin-2 receptor (sIL-2R).

Patients and methods: We examined 15 patients with cancer who received ICIs. Serum sIL-2R levels before and during ICI treatment were measured. The sIL-2R levels of preserved serum samples from another five patients who developed grade 3 irAEs were measured.

Results: Twelve patients showed no significant changes in sIL-2R levels during ICI treatment. Baseline serum sIL-2R levels in three patients increased beyond the normal range before the second cycle. These three patients had grade ≥2 irAEs at the second cycle treatment visit, supporting our hypothesis. Furthermore, at diagnosis of irAEs, the sIL-2R levels of all preserved samples from patients with grade 3 irAEs were significantly elevated.

Conclusion: Serum sIL-2R is a promising biomarker for the diagnosis of irAEs.

Keywords: Immune checkpoint inhibitor; immune-related adverse event; serum soluble interleukin-2 receptor.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antibodies, Monoclonal, Humanized / adverse effects
  • Antibodies, Monoclonal, Humanized / therapeutic use
  • Biomarkers, Tumor / blood*
  • Female
  • Humans
  • Immune Checkpoint Inhibitors / adverse effects*
  • Immune Checkpoint Inhibitors / therapeutic use
  • Ipilimumab / adverse effects
  • Ipilimumab / therapeutic use
  • Male
  • Middle Aged
  • Neoplasms / drug therapy*
  • Neoplasms / immunology
  • Nivolumab / adverse effects
  • Nivolumab / therapeutic use
  • Receptors, Interleukin-2 / blood*
  • Treatment Outcome
  • Up-Regulation

Substances

  • Antibodies, Monoclonal, Humanized
  • Biomarkers, Tumor
  • Immune Checkpoint Inhibitors
  • Ipilimumab
  • Receptors, Interleukin-2
  • Nivolumab
  • pembrolizumab